6-(2-Hydroxy-4-methylcyclohexyl)-2-methylheptane-2,3-diol

Details

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Internal ID 6b06012d-329e-4940-9e36-074c0d3c6a4d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 6-(2-hydroxy-4-methylcyclohexyl)-2-methylheptane-2,3-diol
SMILES (Canonical) CC1CCC(C(C1)O)C(C)CCC(C(C)(C)O)O
SMILES (Isomeric) CC1CCC(C(C1)O)C(C)CCC(C(C)(C)O)O
InChI InChI=1S/C15H30O3/c1-10-5-7-12(13(16)9-10)11(2)6-8-14(17)15(3,4)18/h10-14,16-18H,5-9H2,1-4H3
InChI Key UYYKVTZPZVIVIA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H30O3
Molecular Weight 258.40 g/mol
Exact Mass 258.21949481 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.33
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-(2-Hydroxy-4-methylcyclohexyl)-2-methylheptane-2,3-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9786 97.86%
Caco-2 - 0.6088 60.88%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8358 83.58%
OATP2B1 inhibitior - 0.8487 84.87%
OATP1B1 inhibitior + 0.9366 93.66%
OATP1B3 inhibitior + 0.9682 96.82%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8545 85.45%
P-glycoprotein inhibitior - 0.9272 92.72%
P-glycoprotein substrate - 0.6166 61.66%
CYP3A4 substrate + 0.5086 50.86%
CYP2C9 substrate - 0.8008 80.08%
CYP2D6 substrate - 0.7440 74.40%
CYP3A4 inhibition - 0.8606 86.06%
CYP2C9 inhibition - 0.8474 84.74%
CYP2C19 inhibition - 0.8682 86.82%
CYP2D6 inhibition - 0.9484 94.84%
CYP1A2 inhibition - 0.8886 88.86%
CYP2C8 inhibition - 0.9566 95.66%
CYP inhibitory promiscuity - 0.9627 96.27%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.7384 73.84%
Eye corrosion - 0.9516 95.16%
Eye irritation - 0.8106 81.06%
Skin irritation - 0.5312 53.12%
Skin corrosion - 0.9367 93.67%
Ames mutagenesis - 0.8339 83.39%
Human Ether-a-go-go-Related Gene inhibition - 0.6854 68.54%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6409 64.09%
skin sensitisation + 0.7112 71.12%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.4798 47.98%
Acute Oral Toxicity (c) III 0.8043 80.43%
Estrogen receptor binding + 0.6026 60.26%
Androgen receptor binding - 0.6492 64.92%
Thyroid receptor binding + 0.6302 63.02%
Glucocorticoid receptor binding + 0.5568 55.68%
Aromatase binding - 0.6243 62.43%
PPAR gamma - 0.8235 82.35%
Honey bee toxicity - 0.8575 85.75%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9110 91.10%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.89% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.43% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.17% 98.95%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 92.19% 97.23%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 90.15% 96.47%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.62% 97.09%
CHEMBL2179 P04062 Beta-glucocerebrosidase 88.53% 85.31%
CHEMBL226 P30542 Adenosine A1 receptor 87.44% 95.93%
CHEMBL218 P21554 Cannabinoid CB1 receptor 87.09% 96.61%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 85.83% 95.58%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.75% 85.14%
CHEMBL2996 Q05655 Protein kinase C delta 85.65% 97.79%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.96% 95.89%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 83.43% 95.27%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.86% 93.56%
CHEMBL2094135 Q96BI3 Gamma-secretase 81.59% 98.05%
CHEMBL206 P03372 Estrogen receptor alpha 80.80% 97.64%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162840995
LOTUS LTS0269597
wikiData Q104199098